Review Topical Reference CH3 CHE MsCI OH OMS Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in Sni and Sn2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow.pushing Instructions nrX CH3 : 0 CI: CH3: : CH3 CH3 HCI Submit Answer Retry Entire Group 2 more group attempts remaining Previous Now Draw the major organic product of the reaction shown below. OH + NaH You do not have to consider stereochemistry. Include counter-ions, e.g., Na, 1, in your submission, but draw them in their own separate sketcher Separate structures with + signs from the drop-down menu. ogy to C- *** [1 ChemDoodle OH HC -CH3 HC/ CH3 H Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C=0 double bond is formed with a reduced Cr(IV) compound as the leaving group. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions fo: 0 H ondere H3C-C-CH3 H3C-C-CH3 H H OH H3C + -CH3 H3C CH3 H Cr(VI) compounds are common reagents for the oxidation of alcohols. Primary alcohols are oxidized to carboxylic acids and secondary alcohols are oxidized to ketones. The mechanism involves a reaction similar to the E2 elimination, whereby a C=O double bond is formed with a reduced Cr(IV) compound as the leaving group. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions nn XI :0: TI H3C-C-CH3 A: H H3C CH3 H Previous